# K113316: DCS Lacrimal Stent

- Pathway: 510(k) (Traditional)
- Applicant: Dcs Surgical, Inc.
- Decided: Nov 8, 2012 after 365 days
- Product code: OKS (Lacrimal Stents And Intubation Sets)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K883233 (1988). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061404: Mono-Crawford Naso-Lacrimal Intubation Device, Fci Ophthalmics, Inc. (2006) Summary page 1.
- K030353: Monocanalicular Stents, Lacrimal Intubation Sets, Eagle Vision, Inc. (2003) Summary page 1.
- (no number) Gunther-Weiss Pre-Amendment Jones Tubes: named in the summary without a submission number

## Most influential descendants
- K140290: Stoploss Jones Tube (2014), 0 descendants of its own

## Indications for use
The DCS Lacrimal Stent is intended for use during repair of the lacrimal system for intubation and bypass to canalicular pathologies.

Source page: https://510kreport.com/device/K113316
Methodology: https://510kreport.com/methodology